US5780414A

US5780414A - Method of removing oily substances with hydrogen-terminated fluoropolyethers

Info

Publication number: US5780414A
Application number: US08/810,771
Authority: US
Inventors: Rossella Silvani; Gianfranco Spataro; Giuseppe Marchionni
Original assignee: Ausimont SpA
Current assignee: Solvay Specialty Polymers Italy SpA
Priority date: 1996-03-07
Filing date: 1997-03-05
Publication date: 1998-07-14
Anticipated expiration: 2017-03-05
Also published as: EP0805199A3; JPH09324195A; IT1283202B1; ATE253628T1; ITMI960442A1; DE69725918D1; EP0805199A2; DE69725918T2; ITMI960442A0; EP0805199B1

Abstract

Use of solvents capable of removing oily substances without solubilizing them, consisting of hydrofluoropolyethers having the general formula

HF.sub.2 CO (CF.sub.2 O).sub.n (CF.sub.2 CF.sub.2 O).sub.m CF.sub.2 H

wherein n and m are integers comprised between 0 and 20, excluding when m and n are contemporaneously 0, and having boiling point from 30° to 200° C. and having a molar ratio 0/C comprised between 0.5-1.

Description

The present invention relates to solvents utilizable as cleaning rinsing agents and capable of removing oils, greases, waxes, etc. from surfaces, which show no toxicity and have no impact on the ozone and low impact on the global warming.

More particularly the present invention relates to solvents having the above charateristics which are capable of removing oily substances, greases, waxes, etc. without solubilizing them.

The technical problem to be solved by the present invention regards the need to have available solvents which are not toxic and have the characteristics indicated above. Such problem is particularly felt since the laws of the various countries have banned or are going to ban the use of most solvents, utilized so far, due to impact problems on the ozone.

As examples of solvents which cannot be used any longer due to their impact on the ozone we can mention solvents containing chlorine, chlorofluorocarbons (CFC) and in the future also hydrochlorofluorocarbons (HCFC).

More specifically the technical problem to be solved regards solvents having the above properties and further be capable of removing oily substances without solubilizing them so that the separation processes for the recovery of the solvents only require common mechanical apparatus, such as skimming or filtering, wihout having to resort to more complex and expensive separation processes, such as for instance fractional or azeotropic distillation.

Another characteristic the solvents must have is that they must not be flammable in order not to incur safety, storage and transport problems.

It was felt the need to have available solvents combining the indicated characteristics and at the same time giving performances comparable with those of the clorinated solvents or chlorofluorocarbons currently utilized in washing operations, i.e. the removal of the oily substance being at least 97.0% by weight.

Solvents capable of removing oily substances, without solubilizing them, and this is an object of the present invention, have been unexpectedly and surprisingly found, having general formula

HF.sub.2 CO(CF.sub.2 C).sub.n (CF.sub.2 CF.sub.2 O).sub.m CF.sub.2 H

wherein n and m are integers comprised between 0 and 20, excluding when m and n are contemporaneously 0, and having boiling point from 30° to 200° C. and preferably from 60° to 150° C., and having a molar ratio O/C between 0.5-1.

The above hydrofluoropolyethers are generally constituted by a mixture of components having a different molecular weight with boiling points comprised in the ranges previously indicated.

Hydrofluoropolyethers of the present invention are obtained by means of decarboxylation processes of alkaline salts obtained by hydrolysis and salification of the corresponding acylfluorides, by means of processes known in the art. For instance decarboxylation is carried out in the presence of hydrogen-donor compounds, for instance water, at temperatures of 140°-170° C. and under pressure of at least 4 atm. See for instance patent EP 695775 and the examples reported therein.

Oily substances or greases and waxes based on oily substances which can be removed without solubilization are silicone, fluorosilicone oils or hydrogenated based oils.

Silicone oils are well known and are generally polymethylsiloxanes with different viscosity, for instance from 50 to 30,000 cSt.

Among fluorosilicones, trifluoropropylmethylpolysiloxane, etc. can be mentioned.

By oils having an hydrogenated basis are meant products based on mineral oils derived from petroleum or on synthetic or semi-synthetic oils. Mineral resins, polyalphaolefins, mineral oils such as for instance the dimer ester, can be mentioned.

The results of the present invention are more unexpected if we consider that tests carried out by the Applicant have shown that perfluoropolyethers having perfluoroalkylic terminals --CF₃, --C₂ F₅, --C₃ F₇, and also fluoropolyethers containing only one end hydrogen are not capable of removing oily substances without solubilizing them with results of industrial interest.

It has been found and this is a further object of the invention, in particular that for oils having an hydrogenated basis or derivatives therefrom it is suitable to add to the solvents of the present invention an additive, as defined below, to increase the removal capacity of oily substances.

Additives are polar and liquid substances at the use temperature which must be soluble in the solvent of the invention for at least 1% by weight.

Obviously higher concentrations can be utilized, provided they are within the solubility limits. Usual concentrations are generally comprised between 5-10% by weight.

Among polar substances we can mention alcohols, for instance from 1 to 4 carbon atoms, preferably isopropylic alcohol; ketones among which acetone, methylethylketone, etc. can be mentioned; ethers among which diethylic ether can be mentioned.

The preferred additives are those containing polar groups in compounds comprising carbon and fluorine, for instance in perf luoroalkane or hydrof luoroalkane chains; the number of carbon atoms is generally such as to render the product liquid as indicated above for the solubility.

The preferred compounds are those from 2 to 6 carbon atoms, for instance CF₃ CH₂ OH, (CF₃)₂ CHOH.

Other preferred compounds are polar substances comprising fluorooxyalkylenic units selected from (C₃ F₆ O), (C₂ F₄ O), (CFXO) wherein X is equal to F or CF₃, (CR₁ R₂ CF₂ CF₂ O) wherein R₁ equal to or different from R₂ is H, F, perfluoroalkyl C₁ -C₃.

Compounds can in particular be mentioned having the general formula:

R.sub.f --CFX--L

L--CF.sub.2 --R.sub.f --CF.sub.2 --L

wherein R_f is selected from perfluoroalkanes, hydrofluoroalkanes,

a) --(C₃ F₆ O)_m' (CFXO)_n' -- wherein the unit (C₃ F₆ O) and (CFXO) are pefluorooxyalkylenic units statistically distributed along the chain; m' and n' are integers such as to give products with boiling point generally from 25° and 300° C., preferably higher than that of the solvent of the invention HF₂ CO(CF₂ C)_n (CF₂ CF₂ O)_m CF₂ H and m'/n' is comprised between 5 and 40, when n' is different from 0; X is equal to F or CF₃ ; n' can be also 0;

b) ##STR1## wherein p', q' and t' are integers such as to give products with the boiling point indicated above in a), p'/q' ranges from 5 to 0.3, preferably 2.7-0.5; t' can be 0 and q'/q'+p'+t' lower than or equal to 1/10 and the t'/p' ratio is from 0.2 to 6;

c) --(CR₁ R₂ CF₂ CF₂ O)_n -- wherein R₁ and R₂ have the meaning indicated above and n is an integer such as to give products with the boiling point indicated above in a);

R_f when is monofunctional has an end group of --OR₃ type wherein R₃ is a perfluoroalkyl C₁ -C₃ ;

wherein L is a group containing polar groups, in particular selected from:

--CH₂ OH; --CH₂ OCH₂ CH₂ OH; --CH₂ (OCH₂ CH₂)_n'" OR' wherein n'" is an integer between 2 and 15 and R' is H, CH₃, COCH₃ ; --CONHCH₂ CH₂ OH.

The preferred additive has formula R_f --CFX--L in which R_f has the structure of a).

The fluoropolyethers indicated are obtainable by the processes well known in the art for instance patents U.S. Pat. Nos. 3,665,041, 2,242,218, 3,715,378, and the European patent EP 239,123. The functionalized fluoropolyethers are obtained for instance according to patents EP 148,482, U.S. Pat. No. 3,810,874.

The perfluoroalkanes have in general from 4 to 20 carbon atoms, preferably from 8 to 12; the hydrofluoroalkanes have the same structure of the perfluoroalkanes but have one or more hydrogen at terminal end.

The solvents of the invention allow a removal of oily substances even higher than 97%. The solvent remaining on the substratum is easily removable by evaporation.

The substrata which can be treated with the solvents of the invention are generally both of organic and inorganic type. Metals, ceramic or glass materials, polymeric substrata can be mentioned.

The removal of oily products can be carried out according to known techniques: by immersion or by spray. In case of immersion, the contact between solvent of the invention and the surface to be cleaned can be favoured by utilizing a ultrasonic bath, which allows to remove more effectively also the solid polluting agents.

The following examples are given for illustrative purposes and are not limitative of the scope of the invention.

EXAMPLE 1

De-oiling: removal of oily products

As solvent (HFPE) a product of formula

HF.sub.2 CO(CF.sub.2 C).sub.n (CF.sub.2 CF.sub.2 O).sub.m CF.sub.2 H

was employed, having a boiling range comprised between 100° and 120° C., number average molecular weight Mn=380 and O/C ratio equal to 0.66.

The product consists of a HFPE mixture having different molecular weight.

The capacity of removing oily products was tested according to the following method.

One drop of the oily product is deposited on the bottom of a glass crystallization vessel and HFPE is slowly added letting it flow along the walls of the vessel.

The behaviour of the oily drop is then observed:

if the drop completely comes off from the bottom, the test is to considered positive;

if the drop remains anchored to the bottom, or it only partially comes off, the test is negative.

The de-oiling tests were carried out with the following oils:

MeSilicone oil 50 cSt Dow Corning

MeSilicone oil 500 cSt Dow Corning

FluoroSilicone oil FS1265® Dow Corning

Silicone oil DC 200® Dow Corning

Dearomatized resin D40® Exxon

PAO (polyalphaolefin) 40 cSt Itec®

Diester PRIOLUBE® 3967 Unichem International

The de-oiling tests were carried out by utilizing HFPE both pure and in admixture with a non ionic additive containing fluorine having the formula

CF.sub.3 O(C.sub.3 F.sub.6 O).sub.m' (CFXO).sub.n' CF.sub.2 CH.sub.2 (OCH.sub.2 CH.sub.2).sub.n'" OH

wherein X=F, CF₃, n'"=5-6, m'+n'=4 having number average molecular weight Mn of 1100.

The additive was utilized when only a partial removal of the drop from the HFPE occurred.

The additive concentration employed in Example 1 was equal to 1% by weight.

The non ionic fluorine-containing additive was preferred to polar solvents such as alcohols, ketones to avoid flammability problems. The HFPE/additive mixtures have no Flash Point.

The results of the De-oiling tests are reported in Table 1.

EXAMPLE 2 (comparative)

For comparison purposes de-oiling tests as described above (Example 1) were carried out by utilizing:

PFPE (GALDEN Y) having formula:

CF₃ --(OCF(CF₃)CF₂)_n (OCF₂)_m -OCF₃ having n/m=40 and boiling point=90° C. and number average molecular weight Mn of 460.

PFC having formula C₆ F₁₄ and boiling point of 59° C.

1,1,2-trichlorotrifluoroethane (CFC-113)

The results are reported in Table 1.

EXAMPLE 3

The HFPE of Example 1 was employed to test the capacity of removing silicone oils from ceramic substrata (chip) according to the following method.

A known amount of silicone oil is put uniformly on electronic components.

The electronic components are weighed on analytical balance and then put into contact with the HFPE in question.

After 5 minutes of immersion, the components are dried for 1 hour at room temperature so as to completely remove the solvent and then weighed again.

The result of the test is expressed as percentage of removed oil.

The conditions of the tests are the following:

room temperature 20° C.

oil amount 0.1 g

HFPE amount 30 ml

The employed oils are the following:

MetilSilicone 500

FluoroSilicone FS1265® Dow Corning

Silicone DC200® Dow Corning

The results are reported in Table 2.

EXAMPLE 4 (comparative)

The same removal tests of Example 3 were repeated with the following fluids:

PFPE GALDEN Y of Example 2

1,1,2-trichlorotrifluoroethane (CFC-113)

PFC of Example 2

The results are given in Table 2.

As it can be noted by comparing the results of Example 3 with those of Example 4, the HFPE of the present invention allow to remove silicone oils with an effectiveness comparabale with that of CFC-113.

The HFPE show moreover the great advantage to remove the oil without dissolving it, wherefore HFPE can be recovered by simple filtering. With the usually utilized solvents, oil passes in solution and therefore the only recycle mean of the solvent remains distillation.

              TABLE 1                                                     
______________________________________                                    
                  HFPE     GALDEN Y                                       
                                   PFC  CFC-113                           
OIL       HFPE    +additive                                               
                           (*)     (*)  (*)                               
______________________________________                                    
MeSilicone 50                                                             
          +       +        +       -    #                                 
MeSilicone 500                                                            
          +       +        -       -    #                                 
FS1265    +       +        -       -    #                                 
DC200     +       +        -       -    #                                 
EXXON D40 -       +        -       #    #                                 
PAO       -       +        -       -    #                                 
Ester dimer                                                               
          -       +        -       -    #                                 
______________________________________                                    
 *comparative                                                             
 + removal without solubilization                                         
 - poor or null removal                                                   
 # removal with solubilization

              TABLE 2                                                     
______________________________________                                    
                  GALDEN Y    PFC   CFC-113                               
OIL       HFPE    (*)         (*)   (*)                                   
______________________________________                                    
MeSilicone 500                                                            
          98.7%   62.0%       82.0%  100%                                 
          (+)     (+)         (+)   (#)                                   
FS1265    99.3%   74.0%       23.0% 99.6%                                 
          (+)     (+)         (+)   (#)                                   
DC200     97.2%   49.0%       23.0% 98.9%                                 
          (+)     (+)         (+)   (#)                                   
______________________________________                                    
 (*)comparative                                                           
 (+)removal without solubilization                                        
 (#)removal with solubilization

Claims

We claim:

1. A method of removing oily substances from a substrate, without solubilizing them, comprising contacting the oily substances with a composition consisting essentially of a compound having the general formula

HF.sub.2 CO(CF.sub.2 O).sub.n (CF.sub.2 CF.sub.2 O).sub.m CF.sub.2 H

wherein n and m are integers comprised between 0 and 20, excluding when m and n are contemporaneously 0, and having a boiling point from 30° to 200° C. and a molar ratio O/C comprised between 0.5-1.

2. The method according to claim 1, wherein the boiling point of the compound is comprised between 60° and 150° C.

3. The method according to claim 1, wherein the oily substances are selected from the group consisting of silicone, fluorosilicone oils or oils having an hydrogenated basis.

4. The method according to claim 3, wherein the oils having an hydrogenated basis are selected from the group consisting of mineral oils derived from petroleum, synehetic and semi-synthetic oils.

5. The method according to claim 4, wherein the oils having an hydrogenated basis are selected from the group consisting of mineral resins, polyalphaolefins and minerals oils.

6. The method according to claim 1, further consists essentially of adding organic polar liquid additive to the composition at the employment temperature and said additive is soluble in the compound at least in amounts of 1% by weight.

7. The method according to claim 6, wherein said additive is selected from the group consisting of alcohols, ketones, ethers and from the compounds having carbon and fluorine.

8. The method according to claim 7, wherein the additives having carbon and fluorine are selected from the group consisting of perfluoroalkanes and hydrofluoroalkanes.

9. The method according to claim 7, wherein the additives having carbon and fluorine are selected from polar substances having fluorooxyalkylenic units selected from the group consisting of (C₃ F₆ O), (C₂ F₄ O), (CFXO) wherein X is equal to F or CF₃, (CR₁ R₂ CF₂ CF₂ O) wherein R₁ is equal to or different from R₂ is H, F, perfluoroalkyl C₁ -C₃.

10. The method according to claim 1, wherein said additives are selected from a compound of the formula

R.sub.f --CFX--L

L--CF.sub.2 --R.sub.f --CF.sub.2 --L

wherein R_f is selected from perfluoroalkanes, hydrofluoroalkanes, and

a) --(C₃ F₆ O)_m' (CFXO)_n' --wherein the unit (C₃ F₆ O) and (CFXO) are peflurooxyalkylenic units statistically distributed along the chain; m' and n' are integers such as to give products with a boiling point from about 25° to 300° C., and m'/n' is comprised between 5 and 40, when n' is different from 0; X is equal to F or CF₃ ; n' can be also 0;

b) ##STR2## where X is the same as above wherein p', q' and t' are integers such as to give products with the boiling point indicated above in a), p'/q' ranges from 5 to 0.3; t' can be 0 and q'/q'+p'+t' lower than or equal to 1/10 and the t'/p' ratio is from 0.2 to 6; and

c) --(CR₁ R₂ CF₂ CF₂ O)_n --wherein R₁ and R₂ have the meaning indicated above in a) and n is an integer such as to give products with the boiling point indicated above;

when R_f is monofunctional it has an end group of --OR₃ wherein R₃ is a perfluoroalkyl C₁ --C₃ ;

wherein L is a group containing polar groups.

11. The method according to claim 9, wherein L is selected from the group consisting of: